Canonical Allele Identifier: PA2828530332
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1706401
ClinVar RCV Id: RCV002284931

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361554.1:p.Ala31Ser
CA386776280
NM_001374625.1:c.91G>T